73086-201-30 : NDC 2026 Code

73086-201-30 : Ascorbic Acid,cholecalciferol,.alpha.-tocopherol Acetate,dl-,pyridoxine Hydrochloride,levomefolate Calcium,folic Acid,cyanocobalamin,biotin,calcium Carbonate,iron,potassium Iodide,magnesium Oxide,fish Oil ( Lunatal Dha )

NDC Code : 73086-201-30 – XML Data Format

                    
<?xml version="1.0" encoding="UTF-8"?>
<NDC>
	<NDCCode>
		73086-201-30
	</NDCCode>
	<PackageDescription>
		30 CAPSULE, GELATIN COATED in 1 BOTTLE (73086-201-30) 
	</PackageDescription>
	<NDC11Code>
		73086-0201-30
	</NDC11Code>
	<ProductNDC>
		73086-201
	</ProductNDC>
	<ProductTypeName>
		HUMAN PRESCRIPTION DRUG
	</ProductTypeName>
	<ProprietaryName>
		Lunatal Dha
	</ProprietaryName>
	<ProprietaryNameSuffix/>
	<NonProprietaryName>
		Ascorbic Acid,cholecalciferol,.alpha.-tocopherol Acetate,dl-,pyridoxine Hydrochloride,levomefolate Calcium,folic Acid,cyanocobalamin,biotin,calcium Carbonate,iron,potassium Iodide,magnesium Oxide,fish Oil
	</NonProprietaryName>
	<DosageFormName>
		CAPSULE, GELATIN COATED
	</DosageFormName>
	<RouteName>
		ORAL
	</RouteName>
	<StartMarketingDate>
		20260904
	</StartMarketingDate>
	<EndMarketingDate/>
	<MarketingCategoryName>
		UNAPPROVED DRUG OTHER
	</MarketingCategoryName>
	<ApplicationNumber/>
	<LabelerName>
		Skya Health, LLC
	</LabelerName>
	<SubstanceName>
		ASCORBIC ACID; CHOLECALCIFEROL; .ALPHA.-TOCOPHEROL ACETATE, DL-; PYRIDOXINE HYDROCHLORIDE; LEVOMEFOLATE CALCIUM; FOLIC ACID; CYANOCOBALAMIN; BIOTIN; CALCIUM CARBONATE; IRON; POTASSIUM IODIDE; MAGNESIUM OXIDE; FISH OIL
	</SubstanceName>
	<StrengthNumber>
		60; 1000; 10; 26; 600; 400; 13; 280; 80; 18; 150; 25; 350
	</StrengthNumber>
	<StrengthUnit>
		mg/1; [iU]/1; [iU]/1; mg/1; ug/1; ug/1; ug/1; ug/1; mg/1; mg/1; ug/1; mg/1; mg/1
	</StrengthUnit>
	<Pharm_Classes>
		Analogs/Derivatives [Chemical/Ingredient], Ascorbic Acid [CS], Blood Coagulation Factor [EPC], Calcium [CS], Calculi Dissolution Agent [EPC], Cations, Divalent [CS], Folate Analog [EPC], Folic Acid [CS], Increased Coagulation Factor Activity [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE], Vitamin B 12 [CS], Vitamin B 6 [Chemical/Ingredient], Vitamin B12 [EPC], Vitamin B6 Analog [EPC], Vitamin C [EPC], Vitamin D [CS], Vitamin D [EPC]
	</Pharm_Classes>
	<DEASchedule/>
	<Status>
		Active
	</Status>
	<LastUpdate>
		2026-09-22
	</LastUpdate>
	<PackageNdcExcludeFlag>
		N
	</PackageNdcExcludeFlag>
	<ProductNdcExcludeFlag>
		N
	</ProductNdcExcludeFlag>
	<ListingRecordCertifiedThrough>
		20271231
	</ListingRecordCertifiedThrough>
	<StartMarketingDatePackage>
		20260904
	</StartMarketingDatePackage>
	<EndMarketingDatePackage/>
	<SamplePackage>
		N
	</SamplePackage>
</NDC>

                    
                

NDC XML XSD Schema

                    
<xs:schema attributeFormDefault="unqualified" elementFormDefault="qualified" xmlns:xs="http://www.w3.org/2001/XMLSchema">
  <xs:element name="NDC">
    <xs:complexType>
      <xs:sequence>
        <xs:element type="xs:string" name="NDCCode"/>
        <xs:element type="xs:string" name="PackageDescription"/>
        <xs:element type="xs:string" name="NDC11Code"/>
        <xs:element type="xs:string" name="ProductNDC"/>
        <xs:element type="xs:string" name="ProductTypeName"/>
        <xs:element type="xs:string" name="ProprietaryName"/>
        <xs:element type="xs:string" name="ProprietaryNameSuffix"/>
        <xs:element type="xs:string" name="NonProprietaryName"/>
        <xs:element type="xs:string" name="DosageFormName"/>
        <xs:element type="xs:string" name="RouteName"/>
        <xs:element type="xs:string" name="StartMarketingDate"/>
        <xs:element type="xs:string" name="EndMarketingDate"/>
        <xs:element type="xs:string" name="MarketingCategoryName"/>
        <xs:element type="xs:string" name="ApplicationNumber"/>
        <xs:element type="xs:string" name="LabelerName"/>
        <xs:element type="xs:string" name="SubstanceName"/>
        <xs:element type="xs:string" name="StrengthNumber"/>
        <xs:element type="xs:string" name="StrengthUnit"/>
        <xs:element type="xs:string" name="Pharm_Classes"/>
        <xs:element type="xs:string" name="DEASchedule"/>
        <xs:element type="xs:string" name="Status"/>
        <xs:element type="xs:string" name="LastUpdate"/>
        <xs:element type="xs:string" name="PackageNdcExcludeFlag"/>
        <xs:element type="xs:string" name="ProductNdcExcludeFlag"/>
        <xs:element type="xs:string" name="ListingRecordCertifiedThrough"/>
        <xs:element type="xs:string" name="StartMarketingDatePackage"/>
        <xs:element type="xs:string" name="EndMarketingDatePackage"/>
        <xs:element type="xs:string" name="SamplePackage"/>
      </xs:sequence>
    </xs:complexType>
  </xs:element>
</xs:schema>